FDA 510(k)

MS-39

K-Number: K221601 · 2023-09-01

Decision Date2023-09-01

Product CodeOBO

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MS-39 is a medical device manufactured by C.S.O. S.R.L.. It received FDA 510(k) clearance on 2023-09-01 under approval number K221601. The device is classified under product code OBO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MS-39?

MS-39 is a medical device that received FDA 510(k) clearance on 2023-09-01. It is manufactured by C.S.O. S.R.L.. The 510(k) number is K221601.

When was MS-39 approved by the FDA?

MS-39 received FDA 510(k) clearance on 2023-09-01, under approval number K221601.

What company makes MS-39?

MS-39 is manufactured by C.S.O. S.R.L..

What is the FDA product code for MS-39?

The FDA product code for MS-39 is OBO.

Related Devices (Code: OBO)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.